Search

everythinglearnresearchcommunity

for

Search:↓

Cronkhite-Canada syndrome may be more treatable and less severe than previously thought.

MCTD should be considered in children with recurring muscle issues, lupus-like symptoms, and edema.

The conclusion is that primary scarring alopecia is a complex condition that requires early and accurate diagnosis for effective treatment.

People with lichen planus have higher bad cholesterol and lower good cholesterol, increasing their risk for heart disease.

A woman's hair loss was correctly diagnosed as Lichen planopilaris after initial misdiagnosis, highlighting the usefulness of trichoscopy in diagnosing hair disorders.

The Lanceolate hair-J mutation in mice mimics human hair disorders like Netherton's syndrome.

A 16-year-old boy with lupus had a rare brain artery issue but fully recovered with treatment.

A woman with lupus also developed a severe skin condition linked to a genetic factor.

The document concludes that better tools are needed to measure skin disease severity in dermatomyositis and cutaneous lupus erythematosus, and introduces the DSSI and CLASI as reliable instruments.

Sleeve gastrectomy leads to significant weight loss and health improvements with few complications.

A kidney transplant patient developed leprosy, likely due to immunosuppression and genetic factors, and improved with treatment.

A family was found with both Trichorhinophalangeal syndrome and Loose Anagen Syndrome, suggesting a genetic connection.

Skin issues from chronic graft-versus-host disease greatly affect daily life, needing teamwork between blood and skin doctors.

LED-LLLT helps heal wounds, reduce pain, and regrow hair using specific light wavelengths.

Certain proteins, Lgr5 and Lgr6, are important markers of adult stem cells and are involved in tissue repair and cancer development.

Scalp edema may be a new variant of conditions reacting to scarring alopecia like LPP.

Lichen planus pigmentosus may indicate undetected hepatitis C infection.

The document reports the 19th global case of a rare skin condition in a patient from Colombia.

Early detection and treatment are crucial to prevent irreversible hair loss in Lichen Planopilaris.

Mice with the 'lanceolate hair' mutation have abnormal hair and skin similar to human Netherton's syndrome.

People with lichen planus are more likely to have dyslipidemia, especially higher triglyceride levels.

Early diagnosis and treatment of nail lichen planus in children can prevent permanent nail damage.

Lichen planopilaris may have a genetic link.

Cronkhite-Canada syndrome is rare, has a poor prognosis, and requires early diagnosis and ongoing treatment.

A gene mutation in mice causes severe skin disorder similar to a human condition.

Taking riboflavin and eating less lysine can help some people with a specific genetic disorder avoid brain damage.

The document concludes that skin biopsies, genetic and environmental factors, and specific treatments are important in managing cutaneous lupus erythematosus.

A Doberman Pinscher had a rare form of autoimmune disease causing hair loss and other severe symptoms.

Lenalidomide effectively and safely treats skin symptoms in pediatric lupus, reducing the need for prednisone.

Treatment with methotrexate and prednisolone led to complete hair regrowth and no relapse for 2 years.